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. 2016 Nov 17;3(4):34. doi: 10.3390/vetsci3040034

Figure 1.

Figure 1

Figure 1

Images of Rickettsia buchneri ISO7 clone B8 transformed with shuttle vector pRAM18dRGA to express GFPuv. Transformants were isolated and grown in Ixodes ricinus embryonic cell line IRE11. Panel (A) Island of IRE11 cells containing transformed R. buchneri expressing GFPuv. Image collected 2.5 months after electroporation and rifampicin selection. Infected cells visualized using a fluorescein isothiocyanate (FITC) filter; Panel (B) Phase contrast microscopic appearance of IRE11 cells heavily infected with transformed R. buchneri. Transformed R. buchneri were in the 23rd serial transfer when imaged. Transformants were maintained in cell cultures at high density (1–5 × 106 cells/mL) and were diluted for this image. Infected cells detach; (C) Same field as shown in panel (B) but visualized using fluorescence microscopy with FITC filter; (D) Composite image made by merging images shown in Panels (B,C). All images taken with a Nikon Diaphot fluorescence microscope. Bar equals 40 µm in all panels.